Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
FEMALE
Healthy Volunteers
ID07084727

Retinal Biomarkers for Early Detection of Blood Vessel Dysfunction in Women With Preeclampsia

Led by University Hospital, Antwerp · Updated on 2025-07-24

60

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Pregnancy causes significant changes in a woman's heart and blood vessels to support blood flow between mother and fetus. Preeclampsia, a condition linked to poor placenta function, often begins with high blood pressure and increases the risk of future heart and blood pressure problems. Detecting early changes in blood vessel health is important to provide proper treatment. This study evaluates a new, non-invasive eye test that examines the blood vessels in the retina to identify signs of blood vessel dysfunction in women who have experienced preeclampsia. Participants will undergo several vascular assessments including measuring arterial stiffness, pulse wave velocity, flow-mediated dilation, and retinal vessel response to light. All these tests are designed to study blood vessel function without invasive procedures. Women taking part will have vascular tests such as pulse wave analysis, ultrasound of the elbow artery during blood flow changes, and retinal imaging to see how blood vessels respond. Researchers will measure retinal biomarkers at the start to assess endothelial function. The study is sponsored by University Hospital, Antwerp, and will monitor participants from the beginning of the study period to detect early blood vessel changes after preeclampsia.

CONDITIONS

Brief Title

Identifying Biomarkers for Endothelial Dysfunction in Women With Preeclampsia

Who Can Participate

Age: 18Years - 40Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • At least 18 years old
  • Willing to undergo vascular assessments
  • Signed informed consent
Not Eligible

You will not qualify if you...

  • Unwilling to provide informed consent
  • Open-angle glaucoma
  • Epilepsia
  • Diabetes or gestational diabetes
  • Multiple pregnancies
  • Fetal malformations
  • Hypercholesterolemia
  • Kidney disease
  • Autoimmune disorders
  • Connective tissue diseases
  • Not female or outside age range 18-40 years (implied by gender and age criteria in study details, but explicitly handled in screening questions only and not in exclusion criteria text here, so not included here)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Vascular Assessments

Duration - 1 day

Participants undergo vascular assessments including pulse wave velocity, pulse wave analysis, flow-mediated dilation, fundus photography, and dynamic retinal vessel analysis to evaluate blood vessel function.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

Antwerp University Hospital

Edegem, Antwerp, Belgium, 2650

Actively Recruiting

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Research Team

S

Studies cardiologie

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

1

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